Patterns of formation of the lymphoid tissue of the oesophageal tonsil in ducks at the early stages of the postnatal period of ontogenesis

Svitlana Usenko, Tetiana Mazurkevych, Piotr Kuropka, Zhanna Stegney
Abstract

The relevance of studying the oesophageal tonsil of ducks at the early stages of the postnatal period of ontogenesis is linked to the need to analyse how the levels of structural organisation of its lymphoid tissue are established. In this context, the aim of the research was to determine the localisation and form of the lymphoid tissue of the oesophageal tonsil in Blagovarsky cross broiler ducks from 1 to 240 days of age. Morphometric investigations were carried out and the topography of the oesophageal tonsil was determined in ducks of the studied age groups. Biological material was fixed in a 10% solution of neutral formalin. For histological examination, paraffin blocks were prepared on a sledge microtome and histological sections were obtained, which were stained to reveal the structural features and area of the tissue components of the oesophageal tonsil. It was established that in ducks, the oesophageal tonsil was macroscopically visualised at the transition of the mucous membrane of the caudal part of the oesophagus into the glandular part of the stomach. Changes in its length and width were asynchronous. Up to 5 days of age, the lymphoid tissue of the oesophageal tonsil was represented only by the diffuse form. In ducks aged 10 days and older, primary and secondary nodules appeared. By 15 days of age, the oesophageal tonsil had reached morphofunctional maturity and was characterised by fully developed lymphoid tissue. In day-old ducklings, an infiltration of the glandular portions of the oesophageal glands and the excretory ducts by lymphocytes was observed. With increasing age, intensive colonisation of the epithelium of the oesophageal glands and the excretory ducts by lymphoid cells was recorded. As a result, the lumina of the glands narrowed and transformed into crypt-like openings that opened into the lumen of the oesophagus. The data obtained on the development of the lymphoid tissue of the oesophageal tonsil in broiler ducks during the initial age phases can be used to optimise rearing processes, improve productive performance and refine vaccination strategies to prevent dangerous infectious diseases

Keywords

immune formations; lymphoid nodules; morphometric investigations; poultry; mucous membrane of the oesophagus

Suggested citation
Usenko, S., Mazurkevych, T., Kuropka, P., & Stegney, Zh. (2026). Patterns of formation of the lymphoid tissue of the oesophageal tonsil in ducks at the early stages of the postnatal period of ontogenesis. Ukrainian Journal of Veterinary Sciences, 17(1), 11-30. https://doi.org/10.31548/veterinary1.2026.11
References
  1. Akhand, A.A., & Ahsan, N. (2023). Cells and organs of the immune system. In M.T. Rahman, W. Teughels & J.R. Lamont (Eds.), Immunology for dentistry (pp. 1-12). Hoboken: John Wiley & Sons. doi: 10.1002/9781119893035.ch1.
  2. Ali, H.M., Ali, K.A., & Taha, A.M. (2023). Comparative anatomical, histological, and electron microscopical studies on the cervical region of the esophagus in some birds with different diet habitsJournal of Advanced Veterinary Research, 13(2), 181-187.
  3. ARRIVE. (n.d.). ARRIVE guidelines. Retrieved from https://arriveguidelines.org.
  4. Buhai, L.O. (2008). Peculiarities of the dynamics of macro-microscopic parameters of the esophageal spongy tissue of musk ducks in early postnatal ontogenesisNaukovyi Visnyk Lvivskoho Natsionalnoho Universytetu Veterynarnoi Medytsyny ta Biotekhnolohii Imeni S.Z. Gzhytskoho, 2(37), 16-20.
  5. Capotă, R., Bostănaru-Iliescu, A.C., Ciaușu-Sliwa, D., & Năstasă, V. (2025). Insights into the avian immune system. Romanian Journal of Veterinary Sciences, 58(3), 454-462. doi: 10.59463/rjvs.2025.3.13.
  6. Casteleyn, C., Doom, M., Lambrechts, E., van den Broeck, W., Simoens, P., & Cornillie, P. (2010). Locations of gut-associated lymphoid tissue in the 3-month-old chicken: A review. Avian Pathology, 39(3), 143-150. doi: 10.1080/03079451003786105.
  7. Ceccopieri, C., & Madej, J.P. (2024). Chicken secondary lymphoid tissues – structure and relevance in immunological research. Animals, 14(16), article number 2439. doi: 10.3390/ani14162439.
  8. Davison, F. (2022). The importance of the avian immune system and its unique features. In B. Kaspers, K.A. Schat, T.W. Göbel & L. Vervelde (Eds.), Avian immunology (pp. 1-9). New York: Academic Press. doi: 10.1016/B978-0-12-818708-1.00010-5.
  9. Donmez, H.H., Eken, E., Besoluk, K., & Sur, E. (2012). The histological characteristics and localization of ACP and ANAE positive lymphocytes in the oesophageal tonsil of the duck (Anas platyrhynchos). Avian Biology Research, 5(1), 11-15. doi: 10.3184/175815512X13264771062961.
  10. DSTU EN ISO 13385-1:2018. (2018). Technical requirements for geometric product parameters (GPS). Linear and angular measuring instruments. Part 1: Calipers. Design and metrological characteristics. Retrieved from https://online.budstandart.com/ua/catalog/doc-page.html?id_doc=80498.
  11. Dyshliuk, N.V. (2009). Development of the striated mycosis of chickens in the postnatal period of ontogenesis. Bulletin of Dnipropetrovsk State Agricultural University, 1, 115-118.
  12. El-Naseery, N.I., Mohammed, A.A., Abuel-Atta, A.A., & Ghonimi, W.A.M. (2021). Species-specific differences of the avian oesophagus: Histological and ultrastructural study. Anatomia, Histologia, Embryologia, 50(5), 788-800. doi: 10.1111/ahe.12721.
  13. OIE/WOAH. (n.d.). Standarts. Retrieved from https://www.woah.org/en/what-we-do/standards.
  14. Friedman, A., Elad, O., Cohen, I., & Bar Shira, E. (2012). The gut associated lymphoid system in the post-hatch chick: Dynamics of maternal IgAIsrael Journal of Veterinary Medicine, 67(2), 75-81.
  15. Guralska, S., Kot, T., Gryshuk, H., Zaika, S., & Dubovyi, A. (2023). Effect of chicken infectious bronchitis vaccine on morphogenesis and differentiation of cells in caecal tonsils. Scientific Horizons, 26(6), 9-21. doi: 10.48077/scihor6.2023.09.
  16. Hantusch, B. (2024). Morphological and functional characteristics of blood and lymphatic vessels. In M. Geiger (Ed.), Fundamentals of vascular biology. Learning materials in biosciences (pp. 1-50). Cham: Springer. doi: 10.1007/978-3-031-64591-4_1.
  17. Horalskyi, L.P., Khomych, V.T., & Kononskyi, O.I. (2015). Fundamentals of histological techniques and morphofunctional methods of studies in norm and pathology. Zhytomyr: Polissia.
  18. Indu, V.R., & Lucy, K.M. (2021). Histology and histochemistry of the oesophageal tonsils in White Leghorn chicken. International Journal of Current Microbiology and Appied Sciences,10(6), 304-308. doi: 10.20546/ijcmas.2021.1006.032.
  19. Indu, V.R., Biju, S., Lucy, K.M., & Maya, S. (2020). Histological studies on the oesophageal tonsils of broiler ducks. Journal of Food and Animal Sciences, 1(1), 53-56. doi: 10.51128/jfas.2020.A010.
  20. Jamil, A., Hameed, I., Rizwan, M.U., Fiaz, M., Usmani, M.T., & Shoaib, M. (2024). Avian immune system unveiled: A comprehensive prospective. THE PROGRESS: A Journal of Multidisciplinary Studies, 5(4), 51-64. doi: 10.71016/tp/3d3njw68.
  21. Kadirova, L.V. (2024). Morphofunctional features of intestinal-associated lymphoid tissueInternational Journal of Integrative and Modern Medicine, 2(6), 522-526.
  22. Khomych, V.T., & Usenko S.I. (2013). Morphology of the ostrich egg of ducks aged 25 to 120 daysScientific Bulletin of the National University of Bioresources and Natural Resources of Ukraine. Series: Veterinary Medicine, Quality and Safety of Animal Production, 188(2), 193-197.
  23. Khomych, V.T., & Usenko, S.I. (2012). Morphofunctional features of the ostrich feathered crest of ducks in the early stages of the postnatal period of ontogenesisBulletin of Zhytomyr National Agroecological University, 3(2), 412-415.
  24. Law of Ukraine No. 3447-IV “On the Protection of Animals from Cruelty”. (2006, February). Retrieved from https://zakon.rada.gov.ua/go/3447-15.
  25. Lestari, D., Murtini, S., Ulupi, N., Gunawan, A., & Sumantri, C. (2023). Flow cytometric evaluation of CD4+ and CD8+ T-cell in IPB-D2 chickens with different Newcastle disease antibody titers level. Veterinary World, 16(5), 1161-1164. doi: 10.14202/vetworld.2023.1161-1164.
  26. Logvinova, V., & Oliyar, A. (2021). Histoarchitectonics of lymphoid formations of the mucosa of the small intestine of muscy ducks. Bulletin of Sumy National Agrarian University, 1(52), 31-37. doi: 10.32845/bsnau.vet.2021.1.5.
  27. Mazur, N., & Dyshliuk, N. (2025). Morphological features of immune formations of the avian digestive tract. Scientific Reports of the National University of Life and Environmental Sciences of Ukraine, 21(5), 28-42. doi: 10.31548/dopovidi/5.2025.28.
  28. Mazurkevych, T., & Khomych, V. (2017). Location features of lymphoid tissue in immune formations of the intestine, meckel’s diverticulum and apical diverticula walls in ducks. Scientific Messenger of LNU of Veterinary Medicine and Biotechnologies. Series: Veterinary Sciences, 19(82), 30-35. doi: 10.15421/nvlvet8207.
  29. Mehrzad, J., Shojaei, S., Keivan, F., Forouzanpour, D., Sepahvand, H., Kordi, A., & Hooshmand, P. (2024). Avian innate and adaptive immune components: A comprehensive review. Journal of Poultry Sciences and Avian Diseases, 2(3), 73-96. doi: 10.61838/kman.jpsad.2.3.7.
  30. Nagy, N., Igyárto, B., Magyar, A., Gazdag, E., Palya, V., & Oláh, I. (2005). Oesophageal tonsil of the chicken. Acta Veterinaria Hungarica, 53(2), 173-188. doi: 10.1556/AVet.53.2005.2.3.
  31. Oláh, I., Nagy, N., Magyar, A., & Palya, V. (2003). Esophageal tonsil: A novel gut-associated lymphoid organ. Poultry Science, 82(5), 767-770. doi: 10.1093/ps/82.5.767.
  32. Park, J.I., Cho, S.W., Kang, J.H., & Park, T.E. (2023). Intestinal Peyer’s patches: Structure, function, and in vitro modeling. Tissue Engineering and Regenerative Medicine, 20(3), 341-353. doi: 10.1007/s13770-023-00543-y.
  33. Pendl, H., & Schmidt, R.E. (2024)Lymphatic and hematopoietic system. In R.E. Schmidt, J.D. Struthers & D.N. Phalen (Eds.), Pathology of pet and aviary birds (pp. 307-341). Hoboken: John Wiley & Sons. doi: 10.1002/9781119650522.ch9.
  34. Reznikov, O.H. (2003). General ethical principles of experiments on animals. The first National congress on bioethicsEndocrinology, 8(1), 142-145.
  35. Rochman, M., Kellerman, K., Jankowski, M.P., & Rothenberg, M.E. (2025). The oesophagus as an immune organ. Nature Reviews Gastroenterology & Hepatology, 22, 657-667. doi: 10.1038/s41575-025-01086-4.
  36. Tizard, I.R. (2024). Veterinary immunology-E-book (11th ed.). Amsterdam: Elsevier Health Sciences.
  37. Yıldırım, N. (2024). Histochemical and immunohistochemical investigations on pyloric tonsil in Turkeys (Meleagris gallopavo). Ankara University Faculty of Veterinary Medicine Journal, 71(3), 259-267. doi: 10.33988/auvfd.1242236.
  38. Zeinali, S., Sutton, K., & Vervelde, L. (2024). Distribution and spatiotemporal development of organised lymphoid tissues in the chicken intestinal tract. Developmental & Comparative Immunology, 151, article number 105096. doi: 10.1016/j.dci.2023.105096.